Targeting the mTOR signaling network in cancer

被引:304
作者
Chiang, Gary G.
Abraham, Robert T.
机构
[1] Wyeth, Dept Oncol Discovery, Pearl River, NY 10960 USA
[2] Burnham Inst Med Res, Program Signal Transduct, La Jolla, CA 92037 USA
关键词
D O I
10.1016/j.molmed.2007.08.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The mammalian target of rapamycin [mTOR) is an unconventional protein kinase that is centrally involved in the control of cancer cell metabolism, growth and proliferation. The mTOR pathway has attracted broad scientific and clinical interest, particularly in light of the ongoing clinical cancer trials with mTOR inhibitors. The mixed clinical results to date reflect the complexity of both cancer as a disease target, and the mTOR signaling network, which contains two functionally distinct mTOR complexes, parallel regulatory pathways, and feedback loops that contribute to the variable cellular responses to the current inhibitors. In this review, we discuss the regulatory pathways that govern mTOR activity, and highlight clinical results obtained with the first generation of mTOR inhibitors to reach the oncology clinics.
引用
收藏
页码:433 / 442
页数:10
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